Description
N-Amino-D-proline is a chiral proline derivative supplied at a minimum purity of 95 % for specialised chemical and biochemical research. It is identified by CAS number 10139-05-6, carries the empirical formula C₅H₁₀N₂O₂, and has a molar mass of 130,15 g/mol. Additional physical data include a flash point of 121,3 °C and a boiling point of 277 °C, which assist safe handling assessments and process planning. This listing provides size appropriate for screening, reference standards, and small-scale synthetic or analytical work. Specifications follow the manufacturer description from Carl ROTH, allowing laboratories to cite consistent formula, mass, and thermal values in protocols and reports. As an N-amino-substituted D-proline, the compound is relevant in peptide-related chemistry, ligand design, and studies that require a defined stereochemical scaffold. The compact unit quantity supports economical evaluation while preserving material for confirmatory runs. Clear CAS, formula, and molar-mass labelling streamline inventory control and stoichiometric calculations across chemical and life-science laboratories.
This article is part of Click chemistry, bioconjugation & synthesis reagents, in Biochemicals & reagents.
Key features
- Purity (GC): reported (%)
- Purity (HPLC): reported (%)
- IR-spectrum: corresponds to reference spectrum
- pH value: reported ()
- Assay (TLC): reported (%)
- Content (acidim.): reported (%)
- Assay: reported (%)
- Melting point: reported (°C)
- Colour: reported
- Form: reported
- CAS number: 10139-05-6
- Pack sizes: 5 mg, 10 mg, 25 mg, 50 mg
- Purity: min. 95 %
- Empirical formula: C₅H₁₀N₂O₂
- Molar mass: 130,15 g/mol
- Flash point: 121,3 °C
- Boiling point: 277 °C
- Technical Information Sheet:
- Safety Data Sheet:
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Questions about N-Amino-D-proline, min. 95 %, 5 mg
What is this article?
N-Amino-D-proline, min. 95 %, 5 mg is the article on this page. Luminix Health distributes Carl Roth for laboratory use. It sits in Click chemistry, bioconjugation & synthesis reagents, inside Biochemicals & reagents, in Microbiology lab supplies.
Click and bioconjugation reagents join two molecules under mild conditions, often an azide to an alkyne, or an NHS ester to an amine. The linker length and the reactive group are the specification. They are small bottles of a reactive compound, and moisture often ruins them.
A biochemical is a molecule of life, sold as a reagent: an amino acid, a sugar, a nucleotide, a lipid, an enzyme, an antibiotic. The difference from a bulk chemical is that the use is a biological one, and the impurities that matter are the ones that change that use. An enzyme is specified by activity, not only by mass. An antibiotic is specified by potency. Papers are on PubMed. Structures are on PubChem. Strains and lines that consume these reagents are at ATCC.
Which category should I open next?
The category is Biochemicals & reagents. The sub-category is Click chemistry, bioconjugation & synthesis reagents. The catalogue is Microbiology lab supplies.
Shelves beside this one are Amino acids & peptides, Carbohydrates & sugars, Coenzymes, nucleotides & vitamins, Biochemicals (other), Enzymes & substrates, Antibiotics & antimycotics, Lipids, steroids & fatty acids and Detergents & surfactants.
What should I check before I order?
When this page shows a safety data sheet, use that manufacturer file. Hazard text does not belong in the sales description. For a pack size, a grade or a certificate that is not on the page, send a quote request or contact the team.
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The seven catalogues are Labware, Lab chemicals, Lab instruments, Lab consumables, Chromatography equipment, Lab safety equipment and Life Science & Microbiology.

